Prospects for AstraZeneca's oral Factor D inhibitor danicopan were looking poor after it failed a phase 2 trial in a rare kidney disease in 2020, but a new readout could reinvigorate the drug.
This "Danicopan Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about danicopan for paroxysmal nocturnal hemoglobinuria (PNH) in the seven major markets. A ...
Dublin, Jan. 24, 2024 (GLOBE NEWSWIRE) -- The "Danicopan Emerging Drug Insight and Market Forecast - 2032" report has been added to ResearchAndMarkets.com's offering. The global healthcare industry ...
London, 22 October, 2024 – Alexion, AstraZeneca Rare Disease, has received a positive recommendation for Voydeya® (danicopan), from the National Institute for Health and Care Excellence (NICE), as an ...
WILMINGTON, Del., December 11, 2023--(BUSINESS WIRE)--Positive results from the 24-week and long-term extension (LTE) period of the pivotal ALPHA Phase III trial showed danicopan as add-on to standard ...
(RTTNews) - AstraZeneca (AZN, AZN.L) said that positive results from the 24-week and long-term extension period of the pivotal ALPHA Phase III trial showed danicopan as add-on to standard of care C5 ...
Achillion Pharmaceuticals, Inc. ACHN announced that the European Medicines Agency (EMA) has granted PRIority Medicines (PRIME) designation to its oral factor D inhibitor danicopan (previously ACH-4471 ...
A prespecified interim analysis of the ALPHA phase III trial evaluating danicopan (ALXN2040), an investigational, oral factor D inhibitor, as an add-on to C5 inhibitor therapy Ultomiris (ravulizumab) ...
A prespecified interim analysis of the ALPHA Phase III trial evaluating danicopan (ALXN2040), an investigational, oral factor D inhibitor, as an add-on to C5 inhibitor therapy ULTOMIRIS ® (ravulizumab ...
The first-in-class oral factor D inhibitor danicopan (Voydeya) has been approved for the management of extravascular hemolysis in patients with paroxysmal nocturnal hemoglobinuria (PNH). EVH affects ...
Positive results from the 24-week and long-term extension (LTE) period of the pivotal ALPHA phase III trial showed danicopan as add-on to standard of care C5 inhibitor therapy Ultomiris (ravulizumab) ...